Prevalence of Permanent Neonatal Diabetes in Slovakia and Successful Replacement of Insulin with Sulfonylurea Therapy in KCNJ11 and ABCC8 Mutation Carriers

CONTEXT: Mutations in the KCNJ11 and ABCC8 genes encoding the pancreatic β-cell K(ATP) channel have recently been shown to be the most common cause of permanent neonatal diabetes mellitus (PNDM). Information regarding the frequency of PNDM has been based mainly on nonpopulation or short-term collect...

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Detalhes bibliográficos
Publicado no:J Clin Endocrinol Metab
Main Authors: Stanik, Juraj, Gasperikova, Daniela, Paskova, Magdalena, Barak, Lubomir, Javorkova, Jana, Jancova, Emilia, Ciljakova, Miriam, Hlava, Peter, Michalek, Jozef, Flanagan, Sarah E., Pearson, Ewan, Hattersley, Andrew T., Ellard, Sian, Klimes, Iwar
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7611849/
https://ncbi.nlm.nih.gov/pubmed/17213273
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2006-2490
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